Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs2606345
CYP1A1
0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs3755724
TIMP4 ; SYN2
0.790 0.360 3 12159406 intron variant C/T snv 0.31 8
rs2351299
GABRB1
1.000 0.040 4 47141348 intron variant G/T snv 0.19 2
rs4869682
SLC1A3
1.000 0.080 5 36656616 intron variant T/G snv 0.50 2
rs9444348
NT5E
6 85465856 intron variant G/A snv 0.43 2
rs10974620
SPATA6L ; SLC1A1
9 4557296 intron variant C/G;T snv 1
rs11001109
ADK
10 74683339 intron variant A/G snv 0.68 1
rs1443445
NTRK2
9 84919243 intron variant G/A snv 0.81 1
rs3780645
NTRK2
9 84944879 intron variant C/T snv 5.9E-02 1
rs1010184002
PEX6
0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs886040971
TRPS1
0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs866294686
TRIM8 ; LOC105378460
0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs387907145
ROGDI
0.695 0.440 16 4800548 stop gained G/A snv 36
rs113871094
FBN1
0.683 0.320 15 48465820 stop gained G/A snv 34
rs1559931177
QRICH1
0.827 0.120 3 49047207 stop gained G/A snv 34
rs387907144
ARID1B
0.716 0.600 6 157181056 stop gained C/A;T snv 34